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| Names | |
|---|---|
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Preferred IUPAC name
[1,1′-Bi(cyclopropylidene)]-2,2′-diene | |
| Other names
1,1′-Bi(cycloprop-2-en-1-ylidene)
| |
| Identifiers | |
3D model (
JSmol)
|
|
| ChemSpider | |
PubChem
CID
|
|
CompTox Dashboard (
EPA)
|
|
| |
| |
| Properties | |
| C6H4 | |
| Molar mass | 76.098 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
| |
Triafulvalene or cyclopropenylidenecyclopropene is a fulvalene hydrocarbon with chemical formula C6H4, composed of two linked cyclopropene rings. Triafulvalene has never been isolated, [1] since it can decompose via an isodesmic reaction. [2] However, this molecule is of theoretical significance for theoretical organic chemists, [3][ why?] and its structure, stability, and spectral properties are well-studied.[ citation needed]
See also
References
- ^ Carey, Francis A.; Richard J. Sundberg (2007). Advanced Organic Chemistry: Part A: Structure and Mechanisms. Springer Science & Business Media. pp. 755–787. ISBN 978-0-387448-99-2.
- ^ Neuenschwander, Markus (1986), "Synthetic and NMR spectroscopic investigations of fulvenes and fulvalenes" (PDF), Pure Appl. Chem., 58 (1): 55–66, doi: 10.1351/pac198658010055, S2CID 55312999
- ^ Scott, Anthony P.; Agranat, Israel; Biedermann, P. Ulrich; Riggs, Noel V.; Radom, Leo (1997). "Fulvalenes, Fulvenes, and Related Molecules: An ab Initio Study". The Journal of Organic Chemistry. 62 (7): 2026–2038. doi: 10.1021/jo962407l. ISSN 0022-3263. PMID 11671506.
 | This article about a hydrocarbon is a stub. You can help Wikipedia by expanding it. |
 | This article about theoretical chemistry is a stub. You can help Wikipedia by expanding it. |
|
| |
| Names | |
|---|---|
|
Preferred IUPAC name
[1,1′-Bi(cyclopropylidene)]-2,2′-diene | |
| Other names
1,1′-Bi(cycloprop-2-en-1-ylidene)
| |
| Identifiers | |
3D model (
JSmol)
|
|
| ChemSpider | |
PubChem
CID
|
|
CompTox Dashboard (
EPA)
|
|
| |
| |
| Properties | |
| C6H4 | |
| Molar mass | 76.098 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
| |
Triafulvalene or cyclopropenylidenecyclopropene is a fulvalene hydrocarbon with chemical formula C6H4, composed of two linked cyclopropene rings. Triafulvalene has never been isolated, [1] since it can decompose via an isodesmic reaction. [2] However, this molecule is of theoretical significance for theoretical organic chemists, [3][ why?] and its structure, stability, and spectral properties are well-studied.[ citation needed]
See also
References
- ^ Carey, Francis A.; Richard J. Sundberg (2007). Advanced Organic Chemistry: Part A: Structure and Mechanisms. Springer Science & Business Media. pp. 755–787. ISBN 978-0-387448-99-2.
- ^ Neuenschwander, Markus (1986), "Synthetic and NMR spectroscopic investigations of fulvenes and fulvalenes" (PDF), Pure Appl. Chem., 58 (1): 55–66, doi: 10.1351/pac198658010055, S2CID 55312999
- ^ Scott, Anthony P.; Agranat, Israel; Biedermann, P. Ulrich; Riggs, Noel V.; Radom, Leo (1997). "Fulvalenes, Fulvenes, and Related Molecules: An ab Initio Study". The Journal of Organic Chemistry. 62 (7): 2026–2038. doi: 10.1021/jo962407l. ISSN 0022-3263. PMID 11671506.
|
| This article about a hydrocarbon is a stub. You can help Wikipedia by expanding it. |
|
| This article about theoretical chemistry is a stub. You can help Wikipedia by expanding it. |